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Published on: February 21, 2018
Colony stimulating factors for prophylaxis of chemotherapy-induced neutropenia in children
1The Pharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Rensselaer, NY, USA.
Insights
Granulocyte colony-stimulating factors (G-CSFs) effectively reduce febrile neutropenia in pediatric cancer patients. Standard doses of filgrastim or pegfilgrastim are recommended for prophylaxis, though more research is needed.
Area of Science:
- Pediatric Oncology
- Hematology
Background:
- Febrile neutropenia (FN) is a serious chemotherapy complication increasing infection risk and mortality.
- Granulocyte colony-stimulating factors (G-CSFs) are used to manage neutropenia, but their role in pediatric FN prophylaxis is understudied.
Purpose of the Study:
- To review the efficacy and safety of G-CSFs for primary prophylaxis of FN in pediatric cancer patients.
- To evaluate current G-CSF dosing and administration guidelines in this population.
Main Methods:
- Systematic review of clinical trials published between 2002 and 2021.
- Analysis of G-CSF (filgrastim and pegfilgrastim) dosages and outcomes in pediatric cancer patients.
Main Results:
- Filgrastim (5 mcg/kg/day) reduced fever duration, hospital stay, and antibiotic use in high-risk neuroblastoma patients.
- Pegfilgrastim (100 mcg/kg single dose) demonstrated similar efficacy in preventing FN and infections, with bone pain as a noted side effect.
Conclusions:
- Standard G-CSF doses are appropriate for pediatric cancer patients weighing over 45 kg, administered at least 24 hours post-chemotherapy.
- Further prospective randomized trials are essential to confirm G-CSF efficacy and safety across diverse pediatric cancer types.
Introduction:
Febrile neutropenia (FN) is one of the complications of chemotherapy that can increase the risk of infection and mortality. Granulocyte colony-stimulating factors (G-CSFs) are used in practice to prevent and treat episodes of neutropenia. The use of G-CSFs in children with cancer has not been studied much for primary prophylaxis of FN.
Areas Covered:
Current data suggest that G-CSFs have a similar pharmacokinetic profile in children and adults. Clinical trials published from 2002 to 2021 using G-CSFs in pediatric cancer patients were reviewed. All evaluated clinical trials used a dosage of 5 mcg/kg of filgrastim daily until neutrophil recovery or a single dose of 100 mcg/kg pegfilgrastim. Filgrastim demonstrated the benefit in decreasing the duration of fever, hospital stay, and antibiotic use in high-risk neuroblastoma patients. Pegfilgrastim showed similar efficacy in reducing the occurrence of FN and infections, with bone pain as an adverse effect.
Expert Opinion:
Filgrastim 5 mcg/kg/day or pegfilgrastim 100 mcg/kg single dose is appropriate when given at least 24 hours or after the chemotherapy in pediatric patients who weigh 45 kg or more. More prospective randomized trials are necessary to further investigate the efficacy and safety of G-CSFs in children with different types of cancer.
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